Patent Application
20120295121
The invention pertains to multi-layer coatings useful for providing a decorative and durable mirror-like finish on various types of metal substrates.
One conventional metal surface treatment method is electroplating, which supplies the performances of anti-corrosion, hardness, durability and mirror-like gloss together with other accessorial treatment. However, electroplating is potentially harmful to the environment owing to the large quantity of toxic byproducts and wastes that is generated. The whole process therefore operates at high cost. This limits and blocks the further development of the electroplating industry. The development of alternative techniques for achieving functional mirror-like coating on target metals, including steel Q195-A and zinc alloy #3, which are low cost and environmentally friendly is therefore desirable.
The present invention provides a coating system having at least three layers which is capable of achieving a multiple function mirror-like coating on metals such as steel and zinc alloy (zinc alloy #3 and steel Q 195-A). The three layers include a base coating of epoxy, which provides anti-corrosion protection for metal surfaces and enhances the adhesion of the mirror-like coating which is also applied to the substrate. The decorative mirror-like coating may be formed on the base coating by the reaction of silver salt solution and glucose solution. A surface coating is fabricated on the middle mirror-like coating layer, which protects the mirror-like coating from being oxidized and scratched. The entire coating system is low in cost and easily adaptable to mass production. The processes of coating mixture preparation and the coating layers are all environmentally friendly.
In one embodiment, the invention furnishes a method of providing a substrate with a multi-layer coating, the method comprising the steps of:
Another aspect of the invention provides a substrate having a multi-layer coating on at least one surface, the multi-layer coating comprising a base coating comprised of cured epoxy, a decorative mirror-like coating comprised of silver on top of the base coating, and a surface coating comprised of polysilicone on top of the decorative mirror-like coating.
The process of the present invention is a method of providing multiple layers of coatings to display a mirror-like performance, together with functions of anti-corrosion and anti-scratch. Detailed exemplary procedures for carrying out such method, including the preparation of coating mixtures and the coating of such mixtures on substrates, are described below in the Examples.
Suitable substrates for use in the present invention include, but are not limited to, metal substrates (e.g., steel, zinc alloys). Prior to application of the base coating, one or more initial preparation steps such as surface polishing, surface cleaning and/or surface pretreatment may be carried out. For example, the substrate surface may be polished using an abrasive method such the use of abrasive paper, vibrating grinder or drum grinder. The substrate surface may also be cleaned by contacting the surface with an aqueous surfactant solution while sonicating (i.e., exposing the surface to ultrasound for a period of time, e.g., at least 30 minutes), rinsing the surface with water, contacting the rinsed surface with a volatile organic solvent or mixture of volatile organic solvents (e.g., a mixture of acetone and ethanol) while sonicating (subjecting to ultrasound), rinsing the surface with additional volatile organic solvent, and drying. If so desired, the substrate may be subjected to a pretreatment wherein the surface is contacted with a silane such as gamma-aminopropyl triethoxysilane. The silane or mixture of silanes may be provided in the form of a solution (e.g., a solution in aqueous ethanol). The substrate may be ultrasonicated for a period of time (e.g., at least 10 minutes) while in contact with the silane. The silane-treated surface may then be dried (e.g., in an oven at 110° C. for more than 20 minutes), then cooled to room temperature.
Following any initial preparation steps as described above, an epoxy base coating is formed on the substrate surface. Typically, an epoxy resin is utilized to form the base coating on the substrate surface, wherein the epoxy resin is cured using a solidifier to provide a base coating comprised of cured epoxy.
Any of the epoxy resins known in the art may be utilized in the present invention. Epoxy resins are characterized by the presence of two or more three-membered cyclic ether groups (epoxy groups) per molecule. Particularly useful are diglycidyl ethers of bisphenol A, derived from bisphenol A and epichlorohydrin. Other suitable epoxy resins may include epoxy cresol novolac resins and polynuclear phenol-glycidyl ether-derived resins. Reactive diluents containing a single epoxy group per molecule, such as glycidyl 2-methyiphenyl ether, may be used in combination with the epoxy resin if so desired. Any of the known solidifiers (curing agents) for epoxy resins may be employed, including both catalytic curing agents and coreactive curing agents. Examples of catalytic curing agents include Lewis acid catalysts (e.g., complexes of boron trifluoride with amines or ethers and boron trichloride complexes) and Lewsis base catalysts (e.g., tertiary amines or polyamines converted into tertiary amines upon reaction with epoxide groups). Coreactive curing agents generally contain active hydrogen atoms and include, but are not limited to, polyamines (which may contain aliphatic, aromatic, cycloaliphatic and/or heterocyclic groups, for example), polyaminoamides, polyphenols, polymeric thiols, polycarboxylic acids, and anhydrides.
One or more leveling agents may be used in the base coating composition. Suitable leveling agents include, for example, polyacrylates and silicone-acrylates. The base coating composition may also contain an air release additive (defoaming agent) such as BYK-A530 silicone polymer air release additive and/or a silane coupling agent.
One or more organic solvents may be utilized in the base coating composition as well to serve as a vehicle for the other components. That is, the epoxy resin, solidifier, leveling agent and so forth may be dissolved in an organic solvent or mixture of organic solvents such as alcohols and ketones (e.g., C1-C6 aliphatic alcohols and C3-C6 aliphatic ketones such as acetone, ethanol, butanol, 4-hydroxy-4-methyl-2-pentanone). Preferably, the solvent is relatively volatile (e.g., normal boiling point not more than 100° C.) to facilitate its removal from the base coating composition once the base coating composition has been applied to the substrate surface.
In one embodiment of the invention, the base coating is formed as two layers (a lower layer and an upper layer). The lower layer may be first formed on the substrate surface by applying a lower layer composition comprised of leveling agent, solidifier and solvent (e.g., a ketone and/or alcohol). Before applying to the substrate surface, the lower layer composition may be degassed, by ultrasonication for example. Any suitable coating method may be used, such as brushing, dipping or spraying. The applied coating may then be heated under conditions effective to remove solvent (e.g., 50° C. for at least 6 hours) and provide a dried lower layer. An upper layer composition is then applied to the dried lower layer, using any of the same coating techniques. The upper layer composition may be comprised of epoxy resin, solidifier, leveling agent, reactive diluent and solvent (e.g., alcohol and/or ketone) and may be degassed by ultrasonication prior to application. Following application of the upper layer composition, the coated substrate may again be heated (e.g. 80° C. for at least 4 hours), under conditions effective to both remove solvent and induce curing of the epoxy resin by reaction with the solidifier.
A decorative mirror-like coating is then formed on the base coating by the following procedures. The surface of the base coating may be first cleaned or roughened by contacting the surface with an organic solvent or mixture of organic solvents (e.g., C1-C6 alcohols, C3-C6 ketones, in particular an acetone/ethanol mixture) and then water, suitably by rinsing. The cleaned substrates may then be dried under conditions effective to remove residual volatiles (e.g., in an oven at 90° C., with the substrate thereafter being cooled to room temperature before the next step). A sensitization step to further prepare the coated substrate for application of the mirror-like coating may then be carried out by contacting the base coating surface with an acidic solution containing stannous ions (prepared, for example, by dissolving stannous chloride into aqueous HCl). The coated substrate may, for example, be dipped into the acidic solution, rinsed with water, and then dried (e.g., in an oven at 90° C.).
The decorative mirror-like coating results from the reaction of a soluble amine complex of silver such as [Ag(NH3)2]+, a reducing sugar such as glucose, and an acetylenic compound such as butynediol. As a result of such reaction, the silver complex is converted, at least in part, to metallic silver, which plates onto the substrate surface. The decorative mirror-like coating thus formed is comprised of silver. A solution of the soluble silver complex may be prepared, for example, by dissolving a silver salt such as silver nitrate into water, adding caustic such as sodium hydroxide to form a precipitate, and then adding an amount of ammonium hydroxide effective to dissolve the precipitate (the resulting solution will contain [Ag(NH3)2]+). This solution may then be combined with a solution of reducing sugar (e.g., glucose) which also contains an acidic catalyst such as a carboxylic acid (e.g., citric acid, lactic acid) and a solution of the acetylenic compound (e.g., butynediol). The acetylenic compound solution may be first combined with the sugar solution and the resulting solution then combined with the silver amine complex solution to provide a mirror-like coating composition. The mirror-like coating composition is contacted with the coated substrate by, for example, immersing the coated substrate in the mirror-like coating composition, preferably immediately after such composition has been prepared. Contacting is typically continued for 5 to 10 minutes at approximately room temperature or such other conditions effective to form the desired mirror-like coating on the substrate, generally without stirring or vibration. Thereafter, the substrate may be rinsed with water and dried. If so desired, the mirror-like coating layer may be treated to improve its oxidation resistance by, for example, contacting the mirror-like coating layer with a solution of a thiol such as hexadecanethiol and a surfactant such as an ethoxylated nonylphenol (typically, at 30-50° C. for 1-10 minutes). Thereafter, the substrate may be rinsed with water and dried.
Following the formation of the mirror-like coating layer, a surface coating is formed on such layer to protect the mirror-like coating layer (e.g., from oxidation and scratching). Such surface coating may suitably be based on organic silicon-containing compounds such as silanes and organosilicates. Thus, the protective surface coating may be comprised of polysilicone (i.e., a composition comprised of silicon and oxygen). Organic silicon-containing compounds may be reacted, by hydrolysis and/or condensation reactions for example, to provide the protective coating. Illustrative organic silicon-containing compounds include, for example, silanes, tetraalkyl silicates such as tetraethylsilicate, and alkylalkoxysilanes such as methyltrimethoxysilane. An illustrative example of a suitable silane is 3-glycidoxypropyltrimethoxysilane although other epoxyfunctional silanes as well as other organosilanes having alkoxy substituents and/or substituents with functional groups other than epoxy groups may also be used. The organic silicon-containing compounds may be admixed, combined with water or other liquid medium such as an alcohol, and treated with an acid such as a carboxylic acid (e.g., acetic acid) to provide a surface coating composition. If desired or needed to adjust the appearance of the final coated substrate, a dye (in particular, a violet dye such as tri(4-(dimethylamino)phenyl)methylinium chloride) is also present in the surface coating composition. The substrate having the mirror-like coating thereon is contacted (by immersion, for example) with the surface coating composition for at least one minute, then subsequently heated (e.g., at 100° C. for more than 18 hours) to yield the coated substrate in accordance with the invention.
1. Preparation of Coating Mixtures and Coating Layer with Anti-Corrosive Function.
1) Preparation of pretreatment mixture: Mix Silquest® A1100 (γ-aminopropyl triethoxysilane, product of Crompton) with DI water and ethanol. Stir for more than 10 minutes to obtain a uniform solution.
2) Preparation of base coating mixture with anti-corrosive function:
3) Fabrication of the coating layer with anti-corrosive function (base coating).
1) Preparation of roughening solution: Mix acetone and ethanol at a volume ratio of 1:1 at room temperature. Store the roughening solution in a bottle with a lid.
2) Preparation of sensitizing solution: Add stannous chloride into concentrated hydrochloric acid (36%) at room temperature until the stannous chloride is dissolved. Add DI water to make the concentrations of stannous chloride and hydrochloric acid in the solution 5 g/L and 5 g/L, respectively.
3) Preparation of mirror-like coating solutions: Mirror-like coating solutions include solution A, B and C, in which:
4) Preparation of anti-oxidant solution for mirror-like coating layer: The use of this solution is optional. Dissolve 1-hexadecanethiol into iso-propanol. Stir until the solution is uniform (solution A). Add surfactant of polyoxyethylene (9) nonylphenyl ether (IGEPAL CO-630) into DI water to provide solution B. Mix solution A and B to obtain a uniform solution.
5) Fabrication of mirror-like coating layer.
1) Mix silanes of 3-glycidoxypropyltrimethoxysilane (A187), tetraethylsilicate (TEOS) and methyltrimethoxysilane (MTMS) at room temperature. Sonicate the mixture in an ultrasonic bath for 3 minutes. Add DI water into the above silane mixture at room temperature, and then sonicate for 3 minutes. Add acetic acid into the solution at room temperature, and treat at room temperature for more than 12 minutes. Butan-l-ol is added to dilute the coating product.
2) Violet dye of tris(4-(dimethylamino)phenyl)methylium chloride is added into above anti-scratch coating mixture to adjust the appearance of the coated sample if necessary.
3) Fabrication of the coating layer with anti-scratch function. Immerse the samples coated with the mirror-like coating layer in above anti-scratch coating mixture for more than 1 minute. Heat the samples at 100° C. for more than 18 hours.
This application claims priority to U.S. Provisional Application No. 61/457,727, filed May 20, 2011, and incorporated herein by reference in its entirety for all purposes.
| Number | Date | Country | |
|---|---|---|---|
| 61457727 | May 2011 | US |
